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Grant: Travel Awards - Institute Community Support

Ottawa Hospital Research Institute

$1,000.00

Immunomodulatory exosomes derived from human mesenchymal stem cells for treatment of acute respiratory distress syndrome

EF 2018-19

Résumé
Acute respiratory distress syndrome (ARDS) holds the highest cost of any acute care condition on a per case basis in Canada. For patients who are critically ill, ARDS can be highly fatal. This devastating condition is characterized by severe inflammation which can impair normal gas exchange and result in respiratory failure. Despite decades of research, there are no specific therapies for ARDS and current treatment consists mainly of supportive care. Stemming from evidence that mesenchymal stem cells can treat acute lung injury in animal models, current efforts are looking at the therapeutic potential of these stem cells in patients with ARDS. However, cell therapy is limited by potentially serious adverse events including formation of tumours and blood clots. We believe that small membrane-bound particles released by mesenchymal stem cells, known as exosomes, may have similar beneficial effects in acute inflammation, without the risks of cell delivery. Hence, exosomes represent a potentially safer "cell-free" treatment option. This study aimed to determine the therapeutic effects of mesenchymal stem cell-derived exosomes in both cell and animal models of ARDS. In cell experiments, exosomes improved cell migration. In animal experiments, we treated a mouse model of ARDS with exosomes. As a result, exosomes appear to improve the barrier function of lungs and significantly reduce markers of inflammation. These promising results suggest that exosomes may be a viable therapy for ARDS. Future studies will identify and increase expression of molecules that mediate the protective effects of exosomes to enhance their efficacy. If this cell-free therapy is proven beneficial for ARDS, our research group is ideally positioned to move this potentially life-saving treatment into clinical trials and provide a novel approach to treat this vulnerable patient population in Canada.
Programme
Travel Awards - Institute Community Support
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
391741
Name
Tieu Alvin
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Institute of Circulatory and Respiratory Health
Projecttitle
Immunomodulatory exosomes derived from human mesenchymal stem cells for treatment of acute respiratory distress syndrome
Programtype2
Undefined
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Acute Lung Injury; Acute Respiratory Distress Syndrome; Cell Therapy; Exosomes; Extracellular Vesicles; Ics Travel Awards; Mesenchymal Stem Cell
Abstract
Acute respiratory distress syndrome (ARDS) holds the highest cost of any acute care condition on a per case basis in Canada. For patients who are critically ill, ARDS can be highly fatal. This devastating condition is characterized by severe inflammation which can impair normal gas exchange and result in respiratory failure. Despite decades of research, there are no specific therapies for ARDS and current treatment consists mainly of supportive care. Stemming from evidence that mesenchymal stem cells can treat acute lung injury in animal models, current efforts are looking at the therapeutic potential of these stem cells in patients with ARDS. However, cell therapy is limited by potentially serious adverse events including formation of tumours and blood clots. We believe that small membrane-bound particles released by mesenchymal stem cells, known as exosomes, may have similar beneficial effects in acute inflammation, without the risks of cell delivery. Hence, exosomes represent a potentially safer "cell-free" treatment option. This study aimed to determine the therapeutic effects of mesenchymal stem cell-derived exosomes in both cell and animal models of ARDS. In cell experiments, exosomes improved cell migration. In animal experiments, we treated a mouse model of ARDS with exosomes. As a result, exosomes appear to improve the barrier function of lungs and significantly reduce markers of inflammation. These promising results suggest that exosomes may be a viable therapy for ARDS. Future studies will identify and increase expression of molecules that mediate the protective effects of exosomes to enhance their efficacy. If this cell-free therapy is proven beneficial for ARDS, our research group is ideally positioned to move this potentially life-saving treatment into clinical trials and provide a novel approach to treat this vulnerable patient population in Canada.
Competitiondate
201808
Approvedterm2
1 yr 0 mth
Pinamesdelim
Tieu, Alvin
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Circ &Respiratory Hlth~ $1,000~ $0~